Genetic Predisposition to DiseaseGene-Environment InteractionDisease SusceptibilityPolymorphism, Single NucleotideGenotypeGenetic LinkageAllelesEpistasis, GeneticPolymorphism, GeneticPhenotypeGenetic Association StudiesSerotonin Plasma Membrane Transport ProteinsChromosome MappingEnvironmentAdult ChildrenHaplotypesLod ScoreModels, GeneticLinkage DisequilibriumMicrobial Sensitivity TestsGenome-Wide Association StudyCase-Control StudiesBRCA1 ProteinGene FrequencyGenetic MarkersBRCA2 ProteinGenes, BRCA1PedigreeGenetic TestingChromosomes, Human, Pair 6Microsatellite RepeatsSocial EnvironmentGenome, HumanRisk FactorsMutationAnti-Bacterial AgentsFamily HealthGenetic VariationLife Change EventsGenetic LociChromosomes, Human, Pair 1SchizophreniaGerm-Line MutationAlcoholismGenes, RetinoblastomaChromosomes, Human, Pair 2Age of OnsetHeterozygoteGenetic HeterogeneityBreast NeoplasmsAsian Continental Ancestry GroupMolecular Sequence DataDiabetes Mellitus, Type 1Chromosomes, Human, Pair 13Genes, BRCA2Nuclear FamilyNeoplastic Syndromes, HereditaryPolymerase Chain ReactionChromosomes, Human, Pair 5Retinoblastoma ProteinQuantitative Trait LociEndosomal Sorting Complexes Required for TransportEuropean Continental Ancestry GroupFamilyLupus Erythematosus, SystemicDNA Mutational AnalysisChromosomes, Human, Pair 20Carrier ProteinsChromosomes, Human, Pair 10Drug Resistance, BacterialTranscription FactorsNod2 Signaling Adaptor ProteinDNA-Binding ProteinsX ChromosomeMice, CongenicDrug Resistance, MicrobialChromosomes, Human, Pair 17Protein Tyrosine Phosphatase, Non-Receptor Type 22PsoriasisPenetranceRetinoblastomaBase SequenceSequence Analysis, DNAMice, Inbred C57BLExonsAutistic DisorderHLA-DRB1 ChainsDisease Models, AnimalMultifactorial InheritanceChromosomes, Human, Pair 3Neoplasm ProteinsHLA AntigensOvarian NeoplasmsAntifungal AgentsNeuronal Migration DisordersHeterozygote DetectionCrosses, GeneticDiabetes Mellitus, Type 2Chromosomes, Human, Pair 7Crohn Disease